Your browser doesn't support javascript.
loading
Expression of VEGFR-1 (Flt-1) in breast cancer is associated with VEGF expression and with node-negative tumour stage.
Schmidt, Melanie; Voelker, Hans-Ullrich; Kapp, Michaela; Dietl, Johannes; Kammerer, Ulrike.
Afiliação
  • Schmidt M; Department of Gynaecology and Obstetrics, University of Wuerzburg, Germany. melanie_weigand@hotmail.de
Anticancer Res ; 28(3A): 1719-24, 2008.
Article em En | MEDLINE | ID: mdl-18630531
ABSTRACT

BACKGROUND:

Vascular endothelial growth factor (VEGF) promotes breast cancer progression by inducing angiogenesis via VEGF receptors on endothelial cells but also signals directly through receptors such as VEGFR-1 (Flt-1) expressed on tumour cells. The impact of autocrine signalling loops on treatment with VEGF inhibitors is still unclear. MATERIALS AND

METHODS:

Six breast cancer cell lines were tested for expression of VEGFR-1 by RT-PCR and Western blot. To assess clinical significance, 93 breast cancer lesions were evaluated for expression of VEGF and VEGFR-1 by immunohistochemistry.

RESULTS:

VEGFR-1 mRNA was found in all 6 cell lines, while protein expression was found in 5 cell lines. VEGF was expressed in 60% and VEGFR-1 in 39% of breast cancer specimens. VEGFR-1 expression was associated with VEGF expression and with node-negative tumour stage.

CONCLUSION:

Our data suggest that analysis of VEGF/VEGFR-1 expression might be relevant in identifying patients with different response rates upon treatment with antiangiogenic agents.
Assuntos
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptor 1 de Fatores de Crescimento do Endotélio Vascular / Fator A de Crescimento do Endotélio Vascular Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptor 1 de Fatores de Crescimento do Endotélio Vascular / Fator A de Crescimento do Endotélio Vascular Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2008 Tipo de documento: Article